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A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

People with hidradenitis suppurativa often have lower vitamin D levels, weaker hip bones, and altered bone metabolism markers.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

Nutraceuticals that promote hair growth do not reduce tamoxifen's effectiveness in breast cancer treatment.

Custom skincare can be made based on genes, fewer cats in Lublin have FeLV/FIV than national average, and studies also looked at small water bodies, river pollution, guppy growth, toxins in biochars, palm oil issues, and pumpkin seed oil for hair strength.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

The April 2016 JEADV issue covered various dermatology topics, including psoriasis, psoriatic arthritis, mTOR inhibitors, autoimmune diseases, photodynamic therapy, viral DNA in skin diseases, chronic hand eczema, and female hair loss.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Cantú syndrome is caused by mutations in the ABCC9 gene.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A girl with Evans' syndrome had her low platelet count successfully treated with zanubrutinib.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Oxidative stress worsens PCOS by damaging cells and disrupting metabolism, suggesting antioxidant treatments might help.

The combined treatment effectively managed severe skin issues in Olmsted syndrome.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

TRPV3 in skin cells causes inflammation and cell death.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.